N-Phenyl-1-benzyl-4-piperidylsuccinimide
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- Molecular formula
- C23H26N2O2
- CAS Number
- 2888-49-1
- IUPAC Name
- (3S)-3-(1-benzyl-4-piperidyl)-3-phenyl-piperidine-2,6-dione
- Molecular Weight
- 338.47g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2270g/cm3
- Synonyms
- DEXETIMIDE
Identification
Interesting facts
Interesting Facts about (3S)-3-(1-benzyl-4-piperidyl)-3-phenyl-piperidine-2,6-dione
This intriguing compound, known as a piperidine derivative, holds a significant place in medicinal chemistry due to its potential pharmacological properties. Here are some key points that highlight its importance:
- Structural Diversity: The presence of a piperidine ring fused with various functional groups and side chains showcases the compound's structural diversity. This complexity often correlates with diverse biological activities.
- Potential Therapeutic Applications: Research has suggested that compounds similar to (3S)-3-(1-benzyl-4-piperidyl)-3-phenyl-piperidine-2,6-dione may exhibit efficacy as pharmaceutical agents, particularly in the treatment of neurological disorders.
- Chirality: This compound is chiral, meaning it has an enantiomer, which can lead to different biological effects. In drug design, chirality is a crucial factor in determining the efficacy and safety of compounds.
- Influence on Receptors: Compounds with benzyl and piperidine groups are often investigated for their interactions with neurotransmitter receptors, highlighting their potential role in modulating neurotransmission.
- Research and Development: Ongoing research may reveal more about how modifications to this compound can enhance its therapeutic profiles, making it an exciting subject for further study.
As a compound with promising implications, (3S)-3-(1-benzyl-4-piperidyl)-3-phenyl-piperidine-2,6-dione is a shining example of how structural modifications can lead to significant advancements in medicinal chemistry. Its exploration in both laboratory and clinical settings continues to unveil new possibilities in drug development.